Canonical Allele Identifier: CA495906148

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565346G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531443G>C , CM000678.2:g.66531443G>C	GRCh38
NC_000016.9:g.66565346G>C , CM000678.1:g.66565346G>C	GRCh37
NC_000016.8:g.65122847G>C	NCBI36
NG_016862.1:g.23970C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.144C>G	ENSP00000299697.9:p.Arg48=
ENST00000417693.8:c.258C>G	ENSP00000407469.5:p.Arg86=
ENST00000451102.7:c.219C>G	ENSP00000414334.4:p.Arg73=
ENST00000527284.6:c.256C>G
ENST00000527800.6:c.21C>G	ENSP00000433770.1:p.Arg7=
ENST00000544898.6:c.312C>G MANE Select	ENSP00000440898.2:p.Arg104=
ENST00000567357.6:c.*170C>G	ENSP00000457959.2:n.*170C>G
ENST00000569718.6:c.219C>G	ENSP00000464313.2:p.Arg73=
ENST00000620035.5:c.237C>G	ENSP00000483833.2:p.Arg79=
ENST00000676538.1:c.33-13566C>G
ENST00000677379.1:c.27C>G	ENSP00000503672.1:p.Arg9=
ENST00000677420.1:c.21C>G	ENSP00000504648.1:p.Arg7=
ENST00000677497.1:n.199C>G
ENST00000677555.1:c.21C>G	ENSP00000503331.1:p.Arg7=
ENST00000677715.1:c.21C>G	ENSP00000502950.1:p.Arg7=
ENST00000677739.1:c.55-2376C>G	ENSP00000504644.1:n.55-2376C>G
ENST00000678015.1:c.21C>G	ENSP00000502959.1:p.Arg7=
ENST00000678297.1:c.21C>G	ENSP00000503472.1:p.Arg7=
ENST00000678314.1:c.21C>G	ENSP00000504438.1:p.Arg7=
ENST00000678746.1:c.202C>G	ENSP00000503227.1:n.202C>G
ENST00000679154.1:c.59C>G
ENST00000299697.11:c.312C>G	ENSP00000299697.8:p.Arg104=
ENST00000417693.7:c.384C>G	ENSP00000407469.4:p.Arg128=
ENST00000451102.6:c.438C>G	ENSP00000414334.3:p.Arg146=
ENST00000525974.5:c.21C>G	ENSP00000434594.1:p.Arg7=
ENST00000527284.5:c.219C>G	ENSP00000435312.1:p.Arg73=
ENST00000527800.5:c.21C>G	ENSP00000433770.1:p.Arg7=
ENST00000544898.5:c.312C>G	ENSP00000440898.2:p.Arg104=
ENST00000545043.6:c.237C>G	ENSP00000438143.2:p.Arg79=
ENST00000562484.2:c.21C>G	ENSP00000463326.1:p.Arg7=
ENST00000563369.6:c.21C>G	ENSP00000463560.1:p.Arg7=
ENST00000563478.5:c.21C>G	ENSP00000462341.1:p.Arg7=
ENST00000564917.5:c.312C>G	ENSP00000455187.1:p.Arg104=
ENST00000567357.5:c.*170C>G	ENSP00000457959.1:n.*170C>G
ENST00000569718.5:c.206C>G
ENST00000620035.4:c.258C>G	ENSP00000483833.1:p.Arg86=
NM_001172643.1:c.219C>G	NP_001166114.1:p.Arg73=
NM_001172644.1:c.237C>G	NP_001166115.1:p.Arg79=
NM_001172645.1:c.258C>G	NP_001166116.1:p.Arg86=
NM_001271934.1:c.165C>G	NP_001258863.1:p.Arg55=
NM_001271935.1:c.219C>G	NP_001258864.1:p.Arg73=
NM_001272050.1:c.21C>G	NP_001258979.1:p.Arg7=
NM_004614.4:c.312C>G	NP_004605.4:p.Arg104=
NR_073520.1:n.1591C>G
NM_001172644.2:c.237C>G	NP_001166115.1:p.Arg79=
NM_001271934.2:c.165C>G	NP_001258863.1:p.Arg55=
NM_001272050.2:c.21C>G	NP_001258979.1:p.Arg7=
NM_004614.5:c.312C>G MANE Select	NP_004605.4:p.Arg104=
NR_073520.2:n.1301C>G
NM_001172645.2:c.258C>G	NP_001166116.1:p.Arg86=